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临床试验/2024-513516-99-00
2024-513516-99-00招募中2 期

Durability of Protection After Single Immunisation With Genetically Attenuated Plasmodium Falciparum ∆mei2 (GA2) Sporozoites - a Follow-up, Controlled Human Malaria Rechallenge Study

Leids Universitair Medisch Centrum (LUMC)1 个研究点 分布在 1 个国家目标入组 14 人开始时间: 2024年10月7日最近更新:
干预措施
相关药物

试验速览

阶段
2 期
状态
招募中
发起方
入组人数
14
试验地点
1
主要终点
Protective efficacy

研究概览

简要总结

This study will assess the durability of protection of a single immunisation with the Genetically Attenuated Parasite 2 (GA2) against controlled human malaria infection by rechallenging previously immunised and protected participants from the CoGA study (NCT05468606)

详细描述

This will be a non-randomised, open-label, controlled human malaria infection study that will consist of two study arms: the rechallenge group and infection controls. The rechallenge group consists of study participants from the CoGA study (phase I) who received single immunisation with GA2 and were protected during subsequent CHMI, while infection controls are newly recruited, malaria-naïve study participants. All participants will undergo CHMI through the bites of 5 mosquitos infected with wild-type 3D7 sporozoites. From day 6 to 21 after CHMI, participants will be followed daily on an out-patient basis to determine parasite loads detected by a quantitative polymerase chain reaction (qPCR). As soon as parasitaemia is detected (cut-off >100p/mL), or at the latest 28 days after CHMI, participants will be treated with a curative regimen of antimalarials.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Parallel
主要目的
Prevention
盲法
None

入排标准

年龄范围
18 years 至 64 years(18-64 Years)
接受健康志愿者

入选标准

  • 未提供

排除标准

  • 未提供

研究组 & 干预措施

Rechallenge group

Experimental

Previous CoGA phase 1 study participants who were immunised with GA2 and who did not develop blood-stage malaria during CHMI (protected)

干预措施: CHMI with 3D7 malaria (Biological)

Infection control group

Placebo Comparator

Malaria-naïve participants who have not been previously vaccinated with GA2

干预措施: CHMI with 3D7 malaria (Biological)

结局指标

主要结局

Protective efficacy

时间窗: Moment of CHMI to antimalarial treatment (28 days post CHMI)

Proportion of participants that do not develop parasitaemia (qPCR \>100p/mL) (sterile protection) after CHMI (re)challenge in participants with prior, single GA2 immunisation compared to infection controls.

Time to parasitaemia

时间窗: Moment of CHMI to antimalarial treatment (28 days post CHMI)

The time to parasitaemia (qPCR \>100 p/mL) (prepatent period) after CHMI (re)challenge between participants with prior, single GA2 immunisation and infection controls.

次要结局

  • Cellular immune responses after homologous CHMI rechallenge(Moment of CHMI up to182 days post CHMI)
  • Humoral immune responses after homologous CHMI rechallenge(Moment of CHMI up to182 days post CHMI)

研究者

发起方
Leids Universitair Medisch Centrum (LUMC)
申办方类型
Hospital/Clinic/Other health care facility
责任方
Principal Investigator
主要研究者

Meta Roestenberg

Scientific

Leids Universitair Medisch Centrum (LUMC)

研究点 (1)

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